Deviation Investigator - Sterile GMP Facility
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Proclinical is in the process of building a project team to assist with deviation investigation within an aseptic pharmaceutical manufacturing facility in the Midwestern United States. The client has an outstanding backlog of deviations and are looking to employ the industries best consultants to help with their remediation plans.
We are seeking qualified consultants to join the team who have a background in grade A sterile manufacturing. The successful applicants will have had experience of leading investigations and writing deviations relating to sterile process equipment such as lyophilizers, dry heat ovens, washers, aseptic fillers or autoclaves.
The successful applicants will be degree educated and have experience of working in GMP regulated environment. You should be a strong communicator who is able to influence change at all levels of an organisation. Strong problems solving skills are essential.
The client are paying above market rates and a full expenses package is on offer. The contract will be offered on a 6-month rolling basis and the project can be offered on a W2 or 1099 basis.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Will Hitchcock on +44 203 0789 554 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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